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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827244Generated: October 25, 2026

1,2-Dichloroethane → [1-(2-Phenyl-cyclopropanecarbonyl)-piperidin-4-ylmethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1827244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttrans-2-Phenylcyclopropanecarboxylic acidHCID 237413—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[1-(2-Phenyl-cyclopropanecarbonyl)-piperidin-4-ylmethyl]-carbamic acid tert-butyl esterHCID 23577319—

Reaction Steps

A mixture of tert-butyl piperidin-4-ylmethylcarbamate (Epsilon, 0.80 g, 3.73 mmol), (1R,2R)-2-phenylcyclopropanecarboxylic acid (T. Riley eta al, J. Med. Chem., 15, 1187, 1972) (0.61 g, 3.73 mmol), EDC (1.07 g, 5.60 mmol) and HOBt (0.76 g, 5.60 mmol) in DMF (10 mL) was stirred at RT for 2 h. The reaction mixture was diluted with ethyl acetate (200 mL), washed with aq. sat. NaHCO3 (50 mL), water (5×50 mL), brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel 60 (90 g), eluting with 10:1–10:89–80 CH2Cl2:2-propanol:hexane to give the title compound. (1.22 g, 91.0%). M.S. (M+1): 359.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-85365e70addd4c0c8e7246427abcab01
Source noteuspto-grants-2006_05